• Title/Summary/Keyword: malignant catarrhal fever virus

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Mural folliculitis and alopecia caused by infection with malignant catarrhal fever virus in goat (Capra hircus) (Malignant catarrhal fever virus 감염과 관련된 goat (Capra hircus)의 mural folliculitis와 alopecia)

  • Kim, Ok-Jin;Crawford, Timothy B.
    • Korean Journal of Veterinary Pathology
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    • v.7 no.1
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    • pp.5-9
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    • 2003
  • Malignant catarrhal fever (MCF) is a systemic disease of ruminants caused by a gamma herpesvirus, ovine herpesvirus 2 (OvHV-2). Four 1-year old goats (Capra hircus), which were infected with MCF virus, OvHV-2, by being housed together with MCF virus-infected seep, were referred with a I-month history of chronic dermatitis. On the other hand, MCF virus-negative goats, which were isolated for negative control, had not those kinds of skin problems. Examination of the affected goats revealed generalized alopecia, patchy erythema, and superficial erosions with histologic evidence of mural folliculitis. Fungal culture tests and external parasite tests with the scraping skin samples were negative. However, polymerase chain reaction revealed the existence of MCF virus DNAs in the lesion. These results suggested that MCF virus may induce mural folliculitis and alopecia in goat.

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Development of dot blot hybridization method using non-radio labeled probes for the diagnosis of malignant catarrhal fever (Dot blot hybridization에 의한 malignant catarrhal fever virus의 진단법 개발)

  • Kim, Ok-Jin
    • Korean Journal of Veterinary Pathology
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    • v.7 no.1
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    • pp.1-4
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    • 2003
  • Malignant catarrhal fever (MCF) is a systemic disease of ruminants caused by a gamma herpesvirus, ovine herpesvirus 2 (OvHV-2). Dot blot hybridization (DBH) protocols for detecting and differentiating this MCF virus were developed. OvHV-2 specific primer pairs, 556/555, were used for the amplification of target DNA. Then, the amplified DNA was labeled with incorporation of digoxigenin (DIG). The Dig-labeled probe was able to detect and differentiate specifically OvHV-2 DNA. This DBH technique can be applied to confirm the presence of MCF virus on clinical samples and to differentiate specifically between OvHV-2 infection and other viral infections.

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A Comparative Study of Ultrastructural Changes due to Two Bovine Herpes Viruses (Infectious Bovine Rhinotracheitis Virus and Malignant Catarrhal Fever Virus) (두 종류(種類)의 소의 Herpes Virus에 대한 미세구조변화(微細構造變化)의 비교연구(比較硏究) (소의 전염성비기관염 바이러스와 악성카탈열 바이러스))

  • Seo, Ik Soo
    • Korean Journal of Veterinary Research
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    • v.19 no.1
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    • pp.33-44
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    • 1979
  • Herpes virus인 소의 전염성 비기관염 바이러스와 악성 카탈열 바이러스의 형태(形態)와 그 형성과정(形成過程)(형태발생(形態發生))을 조직배양(組織培養)에서 각기 시험(試驗)하였다. 이 두 종류(種類)의 바이러스는 herpes virus의 특징적(特徵的)인 구조(構造)를 가지나 그 형태발생(形態發生)이 상이(相異)함을 밝혔다. 1. 소의 전염성비기관염(傳染性鼻氣管炎) 바이러스 (IBRV/CT3) 배양에서 그 바이러스의 envelope는 세포질막(細胞質膜)으로부터 유래(由來)됨을 밝혔다. 2. IBRV/CT3 배양에서 envelope는 가진 바이러스는 세포핵내(細胞核內)에는 전혀 나타나지 않았다. 3. 소의 악성(惡性)카탈열(熱) 바이러스(MCFV/C500)의 배양에서 그 바이러스의 envelope는 세포핵막(細胞核膜)으로부터 유래(由來)됨을 밝혔다. 4. 소의 악성(惡性)카탈열(熱) 바이러스(MCFV/C500)에 감염(感染)된 토끼의 폐장(肺臟)에서 얻은 macrophage에 대해 바이러스의 소재(所在)를 추구(追究)한바, 이 바이러스는 macrophage의 세포질내(細胞質內)에만 존재(存在)함을 밝혔다. 그리고 이 바이러스는 탐식(貪食)된 바이러스임을 알았다.

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Development of PCR-dot blot hybridization for the diagnosis of alcelaphine herpesvirus 1 (Alcelaphine herpesvirus 1 진단을 위한 PCR-dot blot hybridization의 개발)

  • Kim, Okjin;Li, Hong
    • Korean Journal of Veterinary Research
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    • v.44 no.1
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    • pp.99-103
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    • 2004
  • The aim of the present study was to develop a sensitive and specific assay for the diagnosis of alcelaphine herpesvirus 1 (AlHV-1) which is a cause agent of malignant catarrhal fever in ruminants. A1HV-1 is a gamma herpesvirus, which is frequent latent, and it is often difficult to detect its antigens or specific nucleic acids because of its low genomic copies in the infected tissues. In this study, polymerase chain reaction (PCR)-dot blot hybridization (DBH) assay for detecting AlHV-1 DNA was developed and evaluated for its sensitivity and specificity as comparison with PCR and DBH alone. The developed PCR-DBH was more sensitive than PCR or DBH alone and also very specific. The results showed that the sensitivity of PCR-DBH were higher and stronger than those of PCR and DBH alone. This PCR-DBH assay can be applied efficiently to confirm the presence of AlHV-1 virus on clinical samples and to differentiate specifically between AlHV-1 infection and other viral infections.